Beckman Coulter, Inc.

Form 483

Chaska, Minnesota, United StatesFEI 2122870Issued June 19, 2013

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2122870.

Observations2

Issue DateJune 19, 2013

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Beckman Coulter, Inc.
Location: Chaska, Minnesota, United States
FEI Number: 2122870
Product Type: Devices
Issue Date: June 19, 2013
Country: United States

Inspection History, 2011 to 2025

NAI2

VAI2

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Beckman Coulter, Inc. FDA Form 483, Chaska, Minnesota, June 19, 2013